A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029132



Internal ID15882318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:39775093..39873242hg38UCSC Ensembl
Innerchr5:39775195..39873344hg19UCSC Ensembl
Innerchr5:39810952..39909101hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3898150
hg1998150
hg1898150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597874
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1029132
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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